Home NDC 81033-005 Kesin MAG-AL
Product NDC 81033-005
11-digit product format 810330005
Labeler code 81033
Product ID 81033-005_515188f8-2cea-822a-e063-6394a90a3a2c
Type HUMAN OTC DRUG
Nonproprietary name Aluminum and Magnesium Hydroxide Suspension
Dosage form SUSPENSION
Route ORAL
Labeler Kesin Pharma Corporation
Application M001
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-11-05
Substance ALUMINUM HYDROXIDE; MAGNESIUM HYDROXIDE
Active strength 200; 200 mg/5mL; mg/5mL
Pharmacologic classes Calculi Dissolution Agent [EPC], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Kesin MAG-AL
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ALUMINUM HYDROXIDE 200 mg/5mL MAGNESIUM HYDROXIDE 200 mg/5mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 5QB0T2IUN0 Internal UNII lookup NBZ3QY004S Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 243463 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 81033-005-01 Kesin MAG-AL 100 in 1 CASE SUSPENSION 100 2 81033-005-30 Kesin MAG-AL 30 mL in 1 CUP, UNIT-DOSE SUSPENSION 30 2
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 24 of 34 · 678 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Extra Strength Antacid Tropical Fruit CALCIUM CARBONATE Harris Teeter, LLC 2c65f7f5-195c-ed33-e063-6294a90a3070 2025-02-11 Warnings Exact identifier application number: M001 Regular Strength Antacid CALCIUM CARBONATE Harris Teeter, LLC 2cb50083-b05f-8aca-e063-6394a90a6d6f 2025-02-11 Warnings Exact identifier application number: M001 Extra Strength Antacid CALCIUM CARBONATE Harris Teeter, LLC 2c544c08-8cdb-edf2-e063-6394a90a024c 2025-02-11 Warnings Exact identifier application number: M001 Extra Strength Antacid Tropical Fruit CALCIUM CARBONATE UNITED NATURAL FOODS, INC. DBA UNFI 1b6a28a2-f848-d185-e063-6294a90ab338 2025-02-07 Warnings Exact identifier application number: M001 Genexa Antacid Maximum Strength CALCIUM CARBONATE Genexa Inc. e4b8f068-ad52-10c8-e053-2a95a90a871f 2025-02-07 Warnings Exact identifier application number: M001 Regular Strength Peppermint Antacid CALCIUM CARBONATE DeMoulas Market Basket 89bdb1c0-df39-4c37-bb0d-0bfd0bff85fb 2025-02-07 Warnings Exact identifier application number: M001 Ultra Strength Antacid CALCIUM CARBONATE UNITED NATURAL FOODS, INC. DBA UNFI 1cbea7c2-fdc0-5a6b-e063-6294a90a9cfa 2025-02-07 Warnings Exact identifier application number: M001 Regular Strength Antacid CALCIUM CARBONATE DeMoulas Market Basket be167e45-3db8-4739-91ac-e83d55223617 2025-02-07 Warnings Exact identifier application number: M001 Extra Strength Smooth Antacid CALCIUM CARBONATE UNITED NATURAL FOODS, INC. DBA UNFI 1b6a4808-4d0b-783c-e063-6394a90af0c3 2025-02-07 Warnings Exact identifier application number: M001 Ultra Strength Antacid Assorted Berries CALCIUM CARBONATE Guardian Drug Company 7f0ca229-7452-4f18-bd2f-bf2dfc3482f8 2025-02-06 Warnings Exact identifier application number: M001 Alkums antacid CALCIUM CARBONATE Guardian Drug Company 7451cd9f-1723-46d0-837e-8dc48bfb6bba 2025-02-06 Warnings Exact identifier application number: M001 Extra Strength Antacid CALCIUM CARBONATE Retail Business Services, LLC. 1e97c054-d6b3-425a-e063-6394a90af836 2025-02-04 Warnings Exact identifier application number: M001 Ultra Strength Antacid Assorted Fruit CALCIUM CARBONATE Retail Business Services, LLC. 214eed56-2d35-8a69-e063-6394a90a1543 2025-02-04 Warnings Exact identifier application number: M001 Ultra Strength Assorted Berry Antacid CALCIUM CARBONATE Harris Teeter, LLC 2bda25ff-9e56-8f8d-e063-6294a90a6a0f 2025-02-04 Warnings Exact identifier application number: M001 Extra Strength Antacid Assorted Fruit CALCIUM CARBONATE Retail Business Services, LLC. 1ea045ae-0b6a-47ae-e063-6394a90a35be 2025-02-04 Warnings Exact identifier application number: M001 Extra Strength Smooth Antacid CALCIUM CARBONATE Retail Business Services, LLC. 214eb054-b7d0-d19f-e063-6394a90a05ba 2025-02-04 Warnings Exact identifier application number: M001 Ultra Strength Antacid Assorted Berries CALCIUM CARBONATE Retail Business Services, LLC. 1e987226-02fa-9c10-e063-6294a90a83bf 2025-02-04 Warnings Exact identifier application number: M001 WONDERBELLY MAXIMUM STRENGTH ANTACID CALCIUM CARBONATE Ginger Health Company 2969ce5b-39ae-47b7-e063-6394a90a1909 2025-02-01 Warnings Exact identifier application number: M001 Sodium Bicarbonate 10 gr (650 mg) SODIUM BICARBONATE CitraGen Pharmaceuticals Inc. 650fa284-5829-588f-e053-2991aa0a9a0e 2025-01-30 Warnings Exact identifier application number: M001 Sodium Bicarbonate 5 gr (325 mg) SODIUM BICARBONATE CitraGen Pharmaceuticals Inc. 68aadbd9-f1c6-8a23-e053-2991aa0afd96 2025-01-30 Warnings Exact identifier application number: M001
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 81033-005-01 81033000501 100 CUP, UNIT-DOSE in 1 CASE (81033-005-01) / 30 mL in 1 CUP, UNIT-DOSE (81033-005-30) 2025-11-05 No No Current 81033-005-30 81033000530 30 mL in 1 CUP, UNIT-DOSE 30 ml Historical